The Paleo- to Mesoproterozoic McArthur Basin and Mount Isa region of northern Australia (Figure 1) is richly-endowed with a range of deposit types (e.g., Ahmad et al., 2013; Geological Survey of Queensland, 2011). These include the basin-hosted base metal (Zn-Pb-Ag) deposits of the North Australian Zinc Belt, the richest zinc province in the world (Geological Survey of Queensland, 2011; Huston et al., 2006), as well as Cu (e.g., Mt Isa Copper) and IOCG (e.g., Ernest Henry) deposits (Geological Survey of Queensland, 2011). The giant size of the base metal deposits makes them attractive exploration targets and significant effort has been undertaken in understanding their genesis and setting and developing methodologies and data sets to aid in further discovery. As part of its Exploring for the Future program, Geoscience Australia is acquiring new, and reprocessing old, data sets to provide industry with new exploration tools for these basin-hosted Zn-Pb and Cu deposits, as well as iron-oxide copper-gold deposits. We have adopted a mineral systems approach (e.g., Huston et al., 2016) focussing on regional aspects such as source rocks, locations of mineral deposits, mineralisation haloes and footprints. Increased understanding of these aspects requires knowledge of the background variability of unaltered rocks within the basin. To assist in this we have undertaken a campaign of baseline geochemical studies, with over 800 new samples collected from sedimentary and igneous units of selected parts of the greater McArthur Basin–Mount Isa region. This has allowed us to document temporal and regional background geochemical (and mineralogical) variation within, and between sedimentary and igneous units. The main focus of this work was directed towards aspects of base metal mineralisation; a concurrent GA study (e.g., Jarrett et al., 2019) looking at aspects of hydrocarbon potential was undertaken in parallel. Appeared in Annual Geoscience Exploration Seminar (AGES) Proceedings, Alice Springs, Northern Territory 24-25 March 2020, p. 105

Manuscript detailing the results of chlorite dissolution experiments conducted at Geoscience Australia.

The stabilities of uranyl-carbonate and uranyl-hydroxide aqueous complexes were experimentally determined at temperatures ranging from 25 to 125 °C using in situ UV–vis and Raman spectroscopic techniques. Combined with earlier determinations of the stability of chloride, sulfate, and hydroxide complexes at temperatures up to 250 °C, these data permit to create a consolidated dataset suitable for modeling of U(VI) mobilization in natural systems. The parameters of the Modified Ryzhenko-Bryzgalin and the Helgeson-Kirkham-Flowers (HKF) Equations of State (EoS) were derived based on this dataset and used for thermodynamic modeling different scenarios of U(VI) mobilization. These models suggest that at conditions relevant to natural systems, carbonate-mediated transport of U(VI) is likely suppressed by the high stability of solid UO2(OH)2 and Na2U2O7. In contrast, sulfate-mediated mobilization mechanisms are highly efficient at acidic and near-neutral pH conditions and can lead to effective hydrothermal mobilization of U(VI). <b>Citation:</b> A. Migdisov, E. Bastrakov, C. Alcorn, M. Reece, H. Boukhalfa, F.A. Capporuscio, C. Jove-Colon, A spectroscopic study of the stability of uranyl-carbonate complexes at 25–150 °C and re-visiting the data available for uranyl-chloride, uranyl-sulfate, and uranyl-hydroxide species, <i>Geochimica et Cosmochimica Acta</i>, 2024, ISSN 0016-7037, https://doi.org/10.1016/j.gca.2024.04.023.

<div>The Birrindudu Basin is a region of focus for the second phase of the Exploring for the Future program (EFTF; 2020–2024) as it contains strata of similar age to the prospective McArthur Basin, South Nicholson region and Mount Isa Province, but remains comparatively poorly understood.</div><div><br></div><div>In order to provide an improved understanding of the stratigraphy, basin architecture and resource potential of the Birrindudu Basin and surrounding region, Geoscience Australia, in collaboration with the Northern Territory Geological Survey and CSIRO is acquiring a range of datasets as part of phase two of EFTF. </div><div><br></div><div>This data release presents XRD results from 79 bulk core samples from the Birrindudu and McArthur basins. This report and the associated analyses were conducted by CSIRO, under contract to Geoscience Australia.</div>

Carbon Capture and Storage (CCS) is a technique for mitigating anthropogenic climate change by separating CO2 from industrial flue gas, transporting it to and storing it in a subsurface geological storage reservoir. The low-salinity (TDS<3 000 mg/L) Jurassic sandstone formations in Australia's Surat Basin have been identified as a potential reservoir system for geological CO2 sequestration. However, given the prevailing use of saline reservoirs in CCS projects elsewhere, limited data are available on CO2-water-rock dynamics during geological sequestration in such low-salinity formations. Here, a combined batch experiment and numerical modelling approach is used to characterise potential CO2-water-rock reaction pathways, to assess potential impacts of CCS on groundwater chemistry, and to identify geochemical tracers of inter- and intra-formational CO2 migration during geological sequestration within the Jurassic sandstones. Mineralogy and physical properties of the prospective reservoir are characterized for 66 core samples from stratigraphic well GSQ Chinchilla 4. Representative samples are reacted with synthetic formation water and high-purity CO2 for up to 27 days at a range of pressures to simulate conditions during carbon sequestration in the Jurassic sandstones. Results show the low formation water salinity, temperature, and mineralization in the reservoirs yield high solubility trapping capacity (1.18 mol/L at 45°C, 100 bar), while the paucity of divalent cations in groundwater and the silicate reservoir matrix result in very low mineral trapping capacity within the footprint of the supercritical CO2 (scCO2) plume. Though alkalinity buffers formation water pH under elevated CO2 pressure, the acidic pH significantly enhances mineral dissolution in reactors with heterogeneous Hutton and Boxvale Sandstone samples. Smaller TDS changes are observed for samples of the mature Precipice Sandstone than for the other formations. Non-radiogenic, regional groundwater-like 87Sr/86Sr values (0.704845 - 0.706600) in batch reactors indicate carbonate and authigenic clay dissolution as the primary reaction pathways regulating solution composition in all formations during carbon sequestration. Slightly higher Sr isotope ratios in felsic samples than in calcitic samples, and dissolved Si concentrations in mature Precipice Sandstone reactors show detrital silicate dissolution to be an ancillary process. Batch reactor degassing at the end of the incubation period was simulated to assess geochemical changes in formation waters during transport away from a scCO2 plume. Model results suggest geological sequestration in the Jurassic sandstone formations would increase regional groundwater alkalinity and redistribute carbonate minerals outside the scCO2 footprint, but is unlikely to result in net mineral trapping of CO2. Several elements are mobilised in concentrations greater than found in regional groundwater, making them viable tracers of CO2 migration. Most notable is cobalt, concentrations of which are significantly elevated regardless of CO2 pressure or sample mineralogy. Experimental results indicate manganese and cadmium concentrations may locally exceed drinking water quality guidelines, but further modelling of intra aquifer mixing is required to quantify the potential risk to regional groundwaters from trace element mobilisation.

<div>The Exploring for the Future (EFTF) program is an Australian government initiative aimed at stimulating investment in resource exploration and development. It operates multiple interconnected projects, such as the Australia’s Resources Framework (ARF), a continental-scale endeavor to enhance understanding of Australia's geology and resource potential. A module of ARF, the Geochemistry for Basin Prospectivity (G4BP), studies Australian basins with prospective base metal mineral systems. </div><div><br></div><div>The current report focuses on the Neoproterozoic segment of the Stuart Shelf region in South Australia, a part of the Adelaide Rift Complex. This research is conducted collaboratively with the Geological Survey of South Australia, examining sediment-hosted copper potential in the rift complex.</div><div><br></div><div>The Adelaide Rift Complex is a geological formation that underwent extensive sedimentation from the Neoproterozoic to early Cambrian, particularly within the rift zone. Stuart Shelf sediments overlay Mesoproterozoic magmatic and Paleoproterozoic metasediment layers. The complex hosts multiple copper deposits, which are usually associated with movement of basinal brines that leach metals from lower basinal layers or rift-related volcanic rocks.</div><div><br></div><div>To improve understanding of the geology of the Stuart Shelf and related copper mineralisation, two primary objectives were set: </div><div><br></div><div>1. Geochemical fingerprinting and baseline data collection: This involves compilation and reanalysis of existing data, along with new data collection aimed at providing comprehensive geochemical data for stratigraphic units within the Stuart Shelf.</div><div><br></div><div>2. Identification of mineral system components: Utilising data from the first objective, this phase aims to identify potential metal and fluid sources and potential sites of metal deposition. </div><div>In conjunction with these efforts, a GA-GSSA geochemical sampling project is underway, tying geochemistry to lithostratigraphic units and facies. The newly acquired geochemical data will be integrated into the overall GSSA-CSIRO project to contribute to a more comprehensive understanding of the sediment-hosted stratabound mineral system.</div><div><br></div>

Paleoproterozoic arc and backarc assemblages accreted to the south Laurentian margin between 1800 Ma and 1600 Ma, and previously thought to be indigenous to North America, more likely represent fragments of a dismembered marginal sea developed outboard of the formerly opposing Australian-Antarctic plate. Fugitive elements of this arc-backarc system in North America share a common geological record with their left-behind Australia-Antarctic counterparts, including discrete peaks in tectonic and/or magmatic activity at 1780 Ma, 1760 Ma, 1740 Ma, 1710-1705 Ma, 1690-1670 Ma, 1650 Ma and 1620 Ma. Subduction rollback, ocean basin closure and the arrival of Laurentia at the Australian-Antarctic convergent margin first led to arc-continent collision at 1650-1640 Ma and then continent-continent collision by 1620 Ma as the last vestiges of the backarc basin collapsed. Collision induced obduction and transfer of the arc and more outboard parts of the Australian-Antarctic backarc basin onto the Laurentian margin where they remained following later breakup of the Neoproterozoic Rodinia supercontinent. North American felsic rocks generally yield Nd depleted mantle model ages consistent with arc and backarc assemblages built on early Paleoproterozoic Australian crust as opposed to older Archean basement making up the now underlying Wyoming and Superior cratons. Appeared in Lithosphere (2019) 11 (4): 551–559, June 10, 2019.

This database contains geochemical data for samples analysed both for inorganic and organic geochemistry. Analytical data are sourced from Geoscience Australia's Inorganic Geochemistry Database (OZCHEM) and Organic Geochemistry Database (ORGCHEM), respectively. The data are joined on a unique sample number. Inorganic geochemical data cover the majority of the periodic table, with metadata on analytical methods and detection limits. Organic geochemical data include results of pyrolysis, derivative calculated values, and, where available, isotopic composition of carbonates (D13C) and isotopic composition of rock nitrogen (D15N). Further, there are provisions for delivery of isotopic data for kerogen (H, C, N) and oxygen (O) for carbonates. Where available, sample descriptions include stratigraphic unit names and ages, and lithology. Location information includes coordinates of the sampled feature (eg, borehole), coordinates of the sample and sample depth. Interpretation of the combined inorganic and organic geochemistry for organic-rich shales will facilitate comprehensive characterisation of hydrocarbons source rocks and mineral commodities source and trap environments. All are achieved within the frameworks of petroleum and mineral systems analysis. The initial data delivered by this service include 1785 samples from 35 boreholes from 14 geological provinces, including recently released data for 442 samples from the South Nicholson National Drilling Initiative Carrara 1 stratigraphic drill hole (Butcher et al., 2021; Carson et al., 2021). Many sampled boreholes are located within the polygon of the Exploring for the Future Barkly-Isa-Georgetown project. This dataset will be updated periodically as more data become available.

<div>The Darling-Curnamona-Delamerian (DCD) project focused on the covered portion of the Delamerian orogen, situated in the south-eastern mainland states of Australia.&nbsp;The aims of the project were to develop a greater understanding of the geodynamic history of the Delamerian Orogen, characterise known magmatic-hydrothermal mineral systems, and assess mineral potential for a suite of minerals including copper (Cu), gold (Au), and nickel (Ni), and critical minerals like platinum-group elements (PGEs) and rare-earth elements (REEs). </div><div>Here, we collate whole rock geochemistry data from new and legacy samples of mafic to intermediate magmatic rocks of the Loch Lilly-Kars Belt in order to determine the likely source of these magmas and constrain the prevailing tectonic setting during their emplacement. We apply multi-elemental diagrams and various elemental discrimination diagrams to characterise various groups of magmatic rocks in these belts, taking into account their geographic affinity and new geochronological data (e.g. Mole et al., 2023; Mole et al., 2024). The geochemical characteristics of these groups and the implications for the tectonic setting into which they were emplaced are discussed. Comparisons are made with potentially similar magmatic rocks of the&nbsp;Koonenberry Belt and Grampians-Stavely Zone. Results from this study have significant implications for the tectonic setting in which the Loch Lilly-Kars Belt developed, and hence also the mineral potential of the Belt. </div><div> </div>

<div>This dataset comprises hydrochemistry results for groundwater, surface water, and rainwater samples collected as part of the Upper Darling Floodplain groundwater study. Associated methods, interpretation, and integration with other datasets are found in the Upper Darling Floodplain geological and hydrogeological assessment (Geoscience Australia Ecat ID:149689). This project is part of the Exploring for the Future (EFTF) program, an eight-year, $225 million Australian Government funded geoscience data and precompetitive information acquisition program. The dataset contains 68 groundwater samples, 17 surface water samples, and four rainwater samples. Groundwater samples are from the Cenozoic formations within the alluvium of the Darling River, the Great Artesian Basin, and the Murray geological basin. Surface water samples are from the Darling River, and rainwater samples were taken within the study area. Subsets of the samples were analysed for major ions and trace metals, stable isotopes of water (δ2H and δ18O), radiocarbon (14C), stable carbon isotopes (δ13C), strontium isotopes (87Sr/86Sr), sulfur hexafluoride (SF6), chlorofluorocarbon (CFC) isotopes, chlorine-36 (36Cl), noble gases, and Radon-222. The results were used to inform a range of hydrogeological questions including aquifer distribution and quality, inter-aquifer connectivity, and groundwater-surface water connectivity.&nbsp;</div><div><br></div>